Effects of alirocumab on types of myocardial infarction : insights from the ODYSSEY OUTCOMES trial
Gislason, Gunnar H/0000-0002-0548-402X; Malynovsky, Yaroslav V/0000-0002-9118-1104; Bhatt, Deepak L./0000-0002-1278-6245; Nikolaev, Konstantin/0000-0003-4601-6203; Sherwood, Matthew/0000-0002-4305-5883; Chumakova, Galina A/0000-0002-2810-6531; Raffel, Owen C/0000-0001-5470-7050; Leonardi, Sergio/0000-0002-4800-6132; Tse, Hung Fat/0000-0002-9578-7808; Reshetko, Olga/0000-0003-3107-7636; Pereira, Helder/0000-0001-8656-4883; Racca, Vittorio/0000-0002-4465-3789; Podoleanu, Cristian/0000-0001-9987-2519; Ersanli, Murat/0000-0003-1847-3087; Muenzel, Thomas/0000-0001-5503-4150; Sandhu, Manjinder/0000-0003-2538-2079; Taskinen, Marja-Riitta/0000-0002-6229-3588; bastos, jose/0000-0002-9526-3123; Manak…
Ethylene oligomerization with 2-hydroxymethyl-5,6,7-trihydroquinolinyl-8-ylideneamine-Ni(II) chlorides
Abstract A series of Ni complexes of the general formula [2-(MeOH)-8-{N(Ar)}C9H8N]NiCl2, where Ar = 2,6-Me2C6H3 in Ni1; 2,6-Et2C6H3 in Ni2; 2,6-i-Pr2C6H3 in Ni3; 2,4,6-Me3C6H2 in Ni4; 2,6-Et2-4-MeC6H2 in Ni5 and 2,4,6-t-Bu3C6H2 in Ni6 has been synthesized and characterized by elemental analysis and IR spectroscopy. On activation with MMAO or Et2AlCl, these complexes showed high activity in ethylene oligomerization, reaching 2.23 × 106 g·mol–1 (Ni) h–1 at 30 °C with the Al/Ni ratio of 5500 and 9.11 × 105 g·mol–1 (Ni) h–1 with the Al/Ni of 800, respectively. Moreover, the content of α-C4 indicated high selectivity exceeding 99% in the Ni/Et2AlCl system. Comparing with the previous report by o…
Nickel(II) complexes with sterically hindered 5,6,7-trihydroquinoline derivatives selectively dimerizing ethylene to 1-butene
A series of nickel complexes bearing N,N-bidentate ligands has been synthesized and characterized by elemental analysis and infrared (IR) spectroscopy. High ethylene dimerization activity, reaching 2.43 × 106 g mol−1(Ni)h−1, was achieved by using these complexes as precatalysts activated with Me2AlCl. Moreover, the selectivity to obtain α-C4 was high (93%–96%). Comparing with the previous report by our group, the higher activity and selectivity may be attributed to the substituent at the 2-position within the ligand, creating the steric hindrance around the metal atom.
CCDC 2124204: Experimental Crystal Structure Determination
Related Article: Wenhua Lin, Ming Liu, Lei Xu, Yanping Ma, Liping Zhang, Zygmunt Flisak, Xinquan Hu, Tongling Liang, Wen‐Hua Sun|2022|Appl.Organomet.Chem.|36|e6596|doi:10.1002/aoc.6596
CCDC 2124203: Experimental Crystal Structure Determination
Related Article: Wenhua Lin, Ming Liu, Lei Xu, Yanping Ma, Liping Zhang, Zygmunt Flisak, Xinquan Hu, Tongling Liang, Wen‐Hua Sun|2022|Appl.Organomet.Chem.|36|e6596|doi:10.1002/aoc.6596